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Napa protein from borrelia burgdorferi

Analyse Napa protein from borrelia burgdorferi in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2PYB
Type
protein
Length
604 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Neutrophil activating protein
UniProt
O51633
Ligands
FE
Pockets
13 · best druggability 0.59

Structure

x-ray diffraction · 1 distinct chain · 60% helix, 0% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, DNeutrophil activating proteinprotein15160% helix, 0% strandO51633

Ligands and binding sites

  • FE · Fe (III) ion · metal · 8 copies · chains A, B, C, D

Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.

Pockets

13 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11330.590.8434empty
22040.560.7921empty
31750.470.7632FE
4730.450.8118empty
5510.440.8416empty

Interfaces

4 interfaces between chains.

  • A–B · 1655 Ų buried · 22 hydrogen bonds · protein-protein
  • C–D · 1650 Ų buried · 22 hydrogen bonds · protein-protein
  • B–C · 649 Ų buried · 7 hydrogen bonds · protein-protein
  • A–C · 470 Ų buried · 2 hydrogen bonds · protein-protein

Compared structures

  • 2PYB · Napa protein from borrelia burgdorferi · the same entry in another collection · chain A against A, TM-score 1.00

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